ARMOR PLAST PVT LTD — Bengaluru
USFDA inspection record for FEI 3005160949, Bengaluru, India.
VAI
Latest classification
2
Inspections on record
3
Form 483 observations on record
History (newest first)
Inspections
26 Feb 2026
VAI — Voluntary action indicated
Compliance: Devices · Devices · FY2026
Form 483: 3 observations
- Analysis of data not used as input for QMS improvement where necessary (ISO 13485:2016 Clause 8.4)
- Document Control Procedure Inadequate (ISO 13485:2016 Clause 4.2.4)
- Information gathered in feedback process not used as input into risk management (ISO 13485:2016 Clause 8.2.1)
Source: FDA Data Dashboard ↗
19 Jan 2023
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3005160949, updated 12 Nov 2026